Clinical Research Coordinator

Cardiovascular Associates of America • Miami, FL

20d • Onsite

About The Position

Cardiovascular Associates of America (CVAUSA) is expanding its clinical trial operations and seeks a Clinical Research Coordinator to support the growth and development of its research program. The coordinator collaborates with clinic staff on existing and new clinical trials and works with teams across CVAUSA’s national network.

The role coordinates and oversees clinical trials and supports research site operations. It involves managing studies with a high degree of autonomy while working closely with investigators, sponsors, and site staff in a fast-paced environment.

Requirements

• Clinical experience in cardiovascular medicine in a licensed role, such as RN, technologist, or medical assistant.
• Minimum of 1–2 years of clinical research experience, including patient enrollment and study coordination.
• Strong organizational and time-management skills.
• Knowledge of GCP, ICH guidelines, and regulatory requirements.
• Ability to manage multiple priorities with accuracy and quality.
• Strong communication skills with sponsors, investigators, site staff, and participants.
• Ability to work independently and as part of a multidisciplinary team.
• Ability to adapt in a dynamic environment and remain focused on study goals.

Nice To Haves

• Bachelor’s degree in a relevant field such as life sciences, healthcare, or clinical research.
• Clinical research certification, such as CCRP.
• Experience with electronic data capture systems and regulatory documentation.

Responsibilities

• Coordinate clinical trials, including patient recruitment, screening, enrollment, and follow-up visits, and ensure study protocols are followed accurately and consistently.
• Support day-to-day research site operations and ensure compliance with regulatory requirements and study protocols.
• Collect, verify, and maintain clinical trial data, ensuring accuracy, completeness, and timely entry.
• Serve as a primary point of contact for study sponsors, participants, and research stakeholders; provide regular study updates and assist with reporting requirements.
• Maintain current study documentation, regulatory binders, and patient records in compliance with GCP, ICH guidelines, and applicable regulations.
• Help identify opportunities to improve research workflows and study performance.

What This Job Offers

• Job Type: Full-time
• Education Level: No Education Listed